Title of article :
Carbazolyl- and diphenylamino substituted fluorenes as hole transport materials
Author/Authors :
Kruzinauskiene، نويسنده , , A. and Matoliukstyte، نويسنده , , A. and Michaleviciute، نويسنده , , A. and Grazulevicius، نويسنده , , J.V. and Musnickas، نويسنده , , J. and Gaidelis، نويسنده , , V. and Jankauskas، نويسنده , , V.، نويسنده ,
Issue Information :
دوماهنامه با شماره پیاپی سال 2007
Pages :
6
From page :
401
To page :
406
Abstract :
Four fluorene-containing aromatic amines with carbazole and diphenylamine moieties were synthesized by Ullmann coupling. Comparative study on their thermal, optical and photoelectrical properties is presented. One synthesized compound is found to form glass with the glass transition temperature 58 °C as characterized by differential scanning calorimetry. The ionization potentials established by electron photoemission technique are in the range 5.9–6.1 eV. Hole-drift mobilities of 50% solid solution of 2,7-dicarbazolyl-9,9-dihexylfluorene in bisphenol Z polycarbonate established by the xerographic time-of-flight technique exceed 10−4 cm2 V−1 s−1 at electric field of 106 V cm−1.
Keywords :
Aromatic amine , Hole-drift mobility , ionization potential
Journal title :
Synthetic Metals
Serial Year :
2007
Journal title :
Synthetic Metals
Record number :
2083966
Link To Document :
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